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1.
Application of a simple model describing regional variations in the contents of manganese and associated minor metals in deep-sea sediments suggests that solid manganese phases are being removed from the <0.5 μm fraction of seawater at ～1–7 · 1012g yr?1 in excess of the rate of stream-supplied manganese. This flux is consistent with: (1) the relative rates of sediment accumulation in the Atlantic and Pacific Oceans; (2) the contrast between the oceanic residence time of manganese calculated from stream-supply data (14 · 103 yr) and from the flux of manganese precipitating in marine sediments or as manganese nodules (0.38–2.4 · 103 yr); (3) the surplus mass of manganese revealed by geochemical balance calculations (22.9 · 102g). On this basis excess manganese is accumulating in deep-sea sediments at 0.2–2.0 · 10?6 g cm?2yr?1. Manganese supplied to the upper layers of marine sediments by diagenesis has been evaluated with the aid of vertical advection—diffusion—reaction models. The calculated diagenetic flux of manganese at the sediment surface in a near-shore environment is in agreement with the known accretion rate of manganese deposits (1.7 · 10?2 g cm?2 10?3 yr?1) and the regionally variable flux over the area assessed is consistent with the presence or absence of manganese nodules at or near the water-sediment interface. The diagenetic flux at the surface of deep-sea sediments has been calculated at 0.7 · 10?4 g cm?2 10?3 yr?1 when the upper, oxic, zone of the sediment is ～20 cm thick. A limiting factor on the in situ production flux of dissolved manganese in deep-sea sediments appears to be the availability of reducing agents for manganese dissolution rather than the rate of downward transport of manganese-rich sediment to a reaction boundary where dissolution takes place. Various estimates of the rate of upward-migrating manganese suggest that manganese precipitates in the oxic zone with a rate constant of ～10?7 sec?1 with the result that diagenetic processes cannot supply the flux of excess manganese through more than ～0.25 m of oxic sediment. However, estimates of the flux of manganese to the oceans by submarine volcanic processes (0.79–1.1 · 1012g yr?1) are similar to the surplus mass of manganese detected by geochemical balance calculations (0.7 · 1012g yr?1). If submarine hydrothermal solutions provide only 10% of this excess then their computed discharge rate (39 g cm?2 yr?1) and residence time in the upper layer of oceanic crust (130,000 yr) agree well with these parameters for continental thermal springs.  相似文献   

2.
Abstract

The rare earth element (REE) distribution in nine deep-sea ferromanganese nodules and their associated siliceous sediments from the Central Indian Ocean Basin (CIOB) have been studied to elucidate the REE relationship among them. Total REE concentration varies from 398–928 ppm in the nodules and 137–235 ppm in the associated sediments, suggesting two- to four-fold enrichment in the nodules compared to associated sediments. REE of nodules and their associated sediments show a positive correlation, suggesting REE are supplied from a common source such as seawater. The positive correlation between REE of nodules and sediments from the CIOB is contrary to the competitive scavenging of REE between nodules and sediment in the equatorial Pacific Ocean. REEs in the nodules are carried by Fe, P, and Ti, whereas in the sediment they are carried by P and Mn phases. A similar REE fractionation pattern with middle REE enrichment over heavy and light REE in both the nodules and their associated sediment suggest fractionation is independent of REE abundance and their carrier phases.  相似文献   

3.
Ferromanganese nodules and crusts contain relatively high concentration of rare earth elements(REE) and yttrium(REY),with a growing interest in exploitation as an alternative to land-based REY resources.On the basis of comprehensive geochemical approach,the abundance and distribution of REY in the ferromanganese nodules from the South China Sea are analyzed.The results indicate that the REY contents in ferromanganese deposits show a clear geographic regularity.Total REY contents range from 69.1×10~(–6) to 2 919.4×10~(–6),with an average value of 1 459.5×10~(–6).Especially,the enrichment rate of Ce content is high,accounting for almost 60% of the total REY.This REE enrichment is controlled mainly by the sorption of ferromanganese oxides and clay minerals in the nodules and crusts.Moreover,the total REY are higher in ferromanganese deposits of hydrogenous origin than of diagenetic origin.Finally,Light REE(LREE) and heavy REE(HREE) oxides of the ferromanganese deposits in the study area can be classified into four grades: non-enriched type,weakly enriched type,enriched type,and extremely enriched type.According to the classification criteria of rare earth resources,the Xisha and Zhongsha platform-central deep basin areas show a great potential for these rare earth metals.  相似文献   

4.
Nitrite is chemically stable but photochemically unstable in seawater. The net disappearance rate in abiotic low-nitrate seawater exposed to sunlight is ～ 10% per day. The primary products are the free radicals NO and OH. Quantitative aspects of the kinetics and secondary product formation are discussed in terms of a fourteen-step reaction scheme. Possible pathways explaining the results are suggested but not unequivocally identified.The rate of reaction in various marine environments is estimated from cruise data and extrapolations to vary between 0.2–60·10?3 moles m?2yr?1, with a suggested global average for comparison purposes of 1–10·103 moles m?2yr?1.These results confirm and quantify our previous suggestion that nitrite photolysis represents a source of OH radical in seawater. The reaction rate is large enough that significant impacts on the geochemical cycles of dissolved organic carbon and nitrogen and heavy metals may plausibly result. Effects on marine biota and atmospheric trace gas composition are also possible. However, specific reactions coupling the nitrite system to other processes have not yet been identified or demonstrated empirically.  相似文献   

5.
The rare earth element (REE) distribution in nine deep-sea ferromanganese nodules and their associated siliceous sediments from the Central Indian Ocean Basin (CIOB) have been studied to elucidate the REE relationship among them. Total REE concentration varies from 398-928 ppm in the nodules and 137-235 ppm in the associated sediments, suggesting two- to four-fold enrichment in the nodules compared to associated sediments. REE of nodules and their associated sediments show a positive correlation, suggesting REE are supplied from a common source such as seawater. The positive correlation between REE of nodules and sediments from the CIOB is contrary to the competitive scavenging of REE between nodules and sediment in the equatorial Pacific Ocean. REEs in the nodules are carried by Fe, P, and Ti, whereas in the sediment they are carried by P and Mn phases. A similar REE fractionation pattern with middle REE enrichment over heavy and light REE in both the nodules and their associated sediment suggest fractionation is independent of REE abundance and their carrier phases.  相似文献   

6.
Thirty-three bulk ferromanganese nodules from the sediment–water interface of siliceous sediment domain from the Central Indian Ocean Basin were analyzed for 50 elements including 6 new (Be, As, Se, Sn, Sb, and Bi) using inductively coupled plasma–mass spectrometer. The Mn/Fe ratio and triangular plot (Fe-Mn-{Cu+Ni+Co?×?10}) suggest that ferromanganese nodules are of hydrogenetic, early diagenetic, and diagenetic origin. In the ferromanganese nodules, Mo, Sb, Bi, and As are highly enriched ～320, 160, 90, and 50 times compared with upper continental crust, respectively. A majority of the elements such as Be, Sc, Ti, V, Co, As, Se, Sr, Y, Zr, Nb, Sn, rare earth elements (REEs), Pb, Bi, P, Th, U, Hf, and Ta are associated with Fe, whereas, Cu, Ni, Zn, Mo, Li, Ga, Sb, Mg, and Cs are associated with Mn in the ferromanganese nodules. Redox proxies such as U/Th (0.14) and Mo/Mn (0.0019) ratio in the ferromanganese nodules suggest their formation under oxic conditions.  相似文献   

7.
南海铁锰结核(壳)的稀土元素地球化学   总被引：10，自引：0，他引：10       下载免费PDF全文
于1987年5—6月间,中、西德在南海进行地球科学调查,获得5个铁锰结壳、6个铁锰结核样品。本文在利用X荧光法测定15个稀土元素的基础上,对南海铁锰结核(壳)的稀土丰度、配分模式与伴生元素的关系以及稀土的来源作了较为详细的探讨。研究表明,南海铁锰结核(壳)的平均丰度为1625×10~(-6),铁锰结核为2167×10~(-6),分别要比太平洋结核高1—2倍,比太平洋北部沉积物高3—4倍,比南海沉积物高10—20倍;结核和结壳的稀土经球粒陨石标准化后的配分模式基本相同,Ce正异常,Eu亏损不明显;与伴生元素、沉积物及岩石稀土对比研究表明,结核(壳)中稀土主要来自南海中酸性岩类风化、淋漓后缓慢沉积。  相似文献   

8.
大洋铁锰结核的微生物成矿过程及其研究进展   总被引：1，自引：1，他引：0  
深海铁锰结核作为世界上潜在的巨大金属宝库已成为当今开发海底矿藏的热点，因而深入了解铁锰结核成矿过程成为其开发利用的先决条件。研究发现多金属铁锰结核中的铁锰矿物不仅仅是由单纯的物理作用形成的，同时也包含了海洋生物驱动的生物矿化的过程。本文介绍了运用分子生物学、矿物学和地球化学等多学科的研究方法对大洋中铁锰的生物成矿过程和成矿特征的研究。深海铁锰结核的生长速率缓慢且其生长演化伴随着微生物群落的活动，因此结核的生长过程同时也记录着不同时期微生物群落结构的变化并生成了大量的微生物化石。在铁和锰的生物矿化过程中，细菌可以通过酶促反应氧化Fe（Ⅱ）和Mn（Ⅱ），同时可能伴随生物能量的生成，此外微生物还可以通过非酶促反应的方式促进Fe和Mn的富集沉淀。这些研究表明生物矿化作用在大洋铁锰结核成矿过程中有巨大贡献，对大洋铁锰结核的生物成因过程提供更加全面准确的理解，从而为今后进一步充实大洋铁锰结核的生物矿化理论及其开发利用提供依据。  相似文献   

9.
A 43 cm long E271 sediment core collected near the East Pacific Rise(EPR) at 13°N were studied to investigate the origin of smectite for understanding better the geochemical behavior of hydrothermal material after deposition.E271 sediments are typical metalliferous sediments. After removal of organic matter, carbonate, biogenic opal,and Fe-Mn oxide by a series of chemical procedures, clay minerals(2 μm) were investigated by X-ray diffraction,chemical analysis and Si isotope analysis. Due to the influence of seafloor hydrothermal activity and close to continent, the sources of clay minerals are complex. Illite, chlorite and kaolinite are suggested to be transported from either North or Central America by rivers or winds, but smectite is authigenic. It is enriched in iron, and its contents are highest in clay minerals. Data show that smectite is most likely formed by the reaction of hydrothermal Fe-oxyhydroxide with silica and seawater in metalliferous sediments. The Si that participates in this reaction may be derived from siliceous microfossils(diatoms or radiolarians), hydrothermal fluids, or detrital mineral phases. And their δ30 Si values are higher than those of authigenic smectites, which implies that a Si isotope fractionation occurs during the formation because of the selective absorption of light Si isotopes onto Feoxyhydroxides. Sm/Fe mass ratios(a proxy for overall REE/Fe ratio) in E271 clay minerals are lower than those in metalliferous sediments, as well as distal hydrothermal plume particles and terrigenous clay minerals. This result suggests that some REE are lost during the smectite formation, perhaps because their large ionic radii of REE scavenged by Fe-oxyhydroxides preclude substitution in either tetrahedral or octahedral lattice sites of this mineral structure, which decreases the value of metalliferous sediments as a potential resource for REE.  相似文献   

10.
The first carbon budget constructed for the Barents Sea to study the fluxes of carbon into, out of, and within the region is presented. The budget is based on modelled volume flows, measured dissolved inorganic carbon (DIC) concentration, and literature values for dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations. The results of the budget show that ～5600±660×106 t C yr?1 is exchanged through the boundaries of the Barents Sea. If a 40% uncertainty in the volume flows is included in the error calculation it resulted in a total uncertainty of ±1600×106 t C yr?1. The largest part of the total budget flux consists of DIC advection (～95% of the inflow and ～97% of the outflow). The other sources and sinks are, in order of importance, advection of organic carbon (DOC+POC; ～3% of both in- and outflow), total uptake of atmospheric CO2 (～1% of the inflow), river and land sources (～0.2% of the inflow), and burial of organic carbon in the sediments (～0.2% of the outflow). The Barents Sea is a net exporter of carbon to the Arctic Ocean; the net DIC export is ～2500±660×106 t C yr?1 of which ～1700±650×106 t C yr?1 (～70%) is in subsurface water masses and thus sequestered from the atmosphere. The net total organic carbon export to the Arctic Ocean is ～80±20×106 t C yr?1. Shelf pumping in the Barents Sea results in an uptake of ～22±11×106 t C yr?1 from the atmosphere which is exported out of the area in the dense modified Atlantic Waters. The main part of this carbon was channelled through export production (～16±10×106 t C yr?1).  相似文献   

11.
This paper deals with the geochemical characteristics of arsenic in sediments from Bohai Gulf. The arsenic in seawater, surface sediments and cores is determined. Also measured are other physical and chemical parameters, such as Ni, Fe, C, pH and Eh in sediments. The values of As range from 0.6 to 4.5 ppb in seawater, from 10.0 to 20.9 ppm in surface sediments and from 6.8 to 22.8 ppm in cores.The contents of As from south are higher than those from north. However the As in sediments is the element not affected by pollution.The adsorption and codeposition of Ferric oxide colloid are the major form of transference of As from seawater to sediments in Bohai Gulf.The valence state of As in sediments is HAsO42-  相似文献   

12.
In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l?1; lindane=54·2 ng l?1; heptachlor=45·0 ng l?1; δ BHC=12·5 ng l?1; aldrin=61·8 ng l?1 and ΣDDT=67·0 ng l?1; and δ BHC=3·2 ng g?1; lindane=4·2 ng g?1 and heptachlor=1·0 ng g?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.  相似文献   

13.
Stoichiometry among bioactive trace metals in the Chukchi and Beaufort Seas   总被引：1，自引：1，他引：0  
The distribution of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb in seawater was investigated in the Chukchi and Beaufort Seas of the western Arctic Ocean in September 2000. The unfiltered and filtered seawater samples were used for determination of total dissolvable metal (TDM) and dissolved metal (DM), respectively. The concentration of labile particulate metal (LPM) was estimated with the difference between that of TDM and DM. The concentrations of TDAl, TDMn, TDFe, TDCo and TDPb varied substantially in the study area. The high concentrations occurred at stations near the Bering Strait, in the Mackenzie delta, and above reductive sediments on the shelf and slope. These elements were mostly dominated by labile particulate species, such as Fe?CMn oxides and species adsorbed on terrestrial clay. DCo was correlated with DMn over the study area (r?=?0.78, n?=?135), and the slope of the regression line was 27 times higher at a pelagic station than at a shelf station. TDNi, TDCu, TDZn and TDCd showed relatively small variations and were generally dominated by dissolved species. There was a moderate correlation between DCd and phosphate for all samples (r?=?0.79), whereas there were no significant correlation between the other DMs and nutrients. TDNi and TDCu showed a remarkable linearity for most stations except those near the Bering Strait (R 2?=?0.95, n?=?126). These results suggest that biogeochemical cycling including uptake by phytoplankton and remineralization from settling particles has only minor control over the distribution of trace metals in this area. Using the present data, the annual input of bioactive trace metals form the Bering Strait and the Mackenzie River was estimated. Also, the trace metal compositions of major water masses were evaluated. The dissolved elemental ratio was P:Al:Mn:Fe:Co:Ni:Cu:Zn:Cd?=?1:1.2?×?10?2:4.4?×?10?4:1.4?×?10?3:3.7?×?10?5:3.7?×?10?3:1.4?×?10?3:4.5?×?10?3:2.2?×?10?4 for Canada Basin deep water (CBDW). This ratio was significantly different from that for Pacific deep water and Bering Sea water, suggesting substantial modification of the trace metal compositions of seawater in the study area.  相似文献   

14.
Said Tlig 《Marine Geology》1982,50(3):257-274
The REE distribution in size fractions of sediments and associated ferromanganese nodules from the Indian Ocean was studied. Bulk-sample patterns of sediments result from the combination of coarsest fractions depleted in Ce and fine fractions enriched in Ce. Ce depletion of the coarsest fractions is related to biogenic silica; on the contrary, REE distribution patterns of fine fractions are closely similar to those of associated ferromanganese nodules. The Ce excess in fine fractions is probably of continental origin, but it could also be derived from submarine weathering of volcanic glass or related to Ce oxydation in the marine environment. In fine fractions Ce is probably in its tetravalent state, hence it can easily be scavenged by fine clays and oxyhydroxydes. Trivalent REE can be incorporated in nodules, partly by occlusion of fine clays or oxyhydroxydes and partly by surface to surface transfer as was proposed by Ehrlich (1968). Comparison between REE patterns of fine-sized fractions, nodules and seawater also supported adsorption as a possible mechanism governing the incorporation of REE of sediments and nodules from seawater. Light REE are probably incorporated as oxyhydroxyde complexes, whereas heavy REE are markedly fractionated with increasing atomic number. This fractionation reflects the complexed form of the heavy REE in seawater.  相似文献   

15.
《Marine Geology》2007,236(1-2):95-119
Lithified crusts located within the sediment and recovered from the Kebrit Deep (Red Sea) are composed of Fe- and Mn-(hydr)oxides, carbonates, and sulfides. Mineralogical and geochemical features of these crusts suggest that they are metalliferous layers lithified by carbonates and formed in the narrow band where the transition zone between the anoxic brine and deep seawater crossed the seafloor. Carbonates cementing the Fe–Mn-(hydr)oxides precipitated from normal saline seawater at T = 20–30 °C. Precipitation of Fe–Mn-(hydr)oxides was superimposed the carbonate precipitation in the transition zone. A pumping mechanism involving cyclic Fe- and Mn-(hydr)oxide precipitation/redissolution operated through the transition zone and produced an enrichment of a number of elements in the crusts. The microbiota played an important role in the geochemical cycle of the elements through the redoxcline and in the mineralogy of the sediments underlying the redoxcline waters. Diagenetic processes led to formation of bi- and ternary carbonates, and disulfides.  相似文献   

16.
The contents of oxyanionic elements (V, Se and Mo) and cationic transition metals (Mn, Fe, Co, Ni, Cu and Zn) in sediments from near-shore to deep-sea environments were measured to clarify factors regulating the distribution of these elements in marine sediments. For cationic transition metals of which contents increase from near-shore to deep-sea environments, the chemical composition of pelagic clays is modeled by a mixture of aluminosilicates having the chemical composition of average shale and Fe–Mn oxides having the chemical composition of associated manganese nodules. The content of V is fairly constant in sediments from near-shore to deep-sea areas. The mixture model of average shale and manganese nodules holds also for V, although most of the V is located in the aluminosilicate lattices. The content of Se in the near-shore sediments is higher and that in the deep-sea sediments is lower than that in average shale. The high content in the near-shore sediments is interpreted as the addition of biogenic materials to aluminosilicates with average shale composition and the low content in deep-sea sediments is explained by oxidative release of Se from aluminosilicates. The content of Mo in sediments increases from near-shore to deep-sea environments. The general distribution of Mo in marine sediments is expressed by the mixture model. An anomalously high content of Mo in a near-shore sediment is attributed to adsorption of molybdate on manganese oxides.  相似文献   

17.
The flux of ammonia, phosphate, silica and radon-222 from Potomac tidal river and estuary sediments is controlled by processes occurring at the sediment-water interface and within surficial sediment. Calculated diffusive fluxes range between 0·6 and 6·5 mmol m?2 day?1 for ammonia, 0·020 and 0·30 mmol m?2 day?1 for phosphate, and 1·3 and 3·8 mmol m?2 day?1 for silica. Measured in situ fluxes range between 1 and 21 mmol m?2 day?1 for ammonia, 0·1 and 2·0 mmol m?2 day?1 for phosphate, and 2 and 19 mmol m?2 day?1 for silica. The ratio of in situ fluxes to diffusive fluxes (flux enhancement) varied between 1·6 and 5·2 in the tidal river, between 2·0 and 20 in the transition zone, and from 1·3 to 5·1 in the lower estuary. The large flux enhancements from transition zone sediments are attributed to macrofaunal irrigation. Nutrient flux enhancements are correlated with radon flux enhancements, suggesting that fluxes may originate from a common region and that nutrients are regenerated within the upper 10–20 cm of the sediment column.The low fluxes of phosphate from tidal viver sediments reflect the control benthic sediment exerts on phosphorus through sorption by sedimentary iron oxyhydroxides. In the tidal river, benthic fluxes of ammonia and phosphate equal one-half and one-third of the nutrient input of the Blue Plains sewage treatment plant. In the tidal Potomac River, benthic sediment regeneration supplies a significant fraction of the nutrients utilized by primary producers in the water column during the summer months.  相似文献   

18.
本文研究了盐场海芽孢杆菌(Marinibacilluscampisalis)与大洋铁锰结核的相互作用过程,以及海洋微生物在铁锰结核形成中的作用。实验选取从深海沉积物中分离培养的盐场海芽孢杆菌(Marinibacillus campisalis)和大洋铁锰结核样品进行相互作用实验,设置有菌组和无菌组,培养过程中间隔取样分析。运用X射线荧光光谱(XRF)分析测定大洋铁锰结核元素组成,通过电感耦合等离子体发射光谱(ICP-OES)和电感耦合等离子体质谱(ICP-MS)测定反应过程中Fe、Mn、Co、Ni、Cu等离子浓度的变化,通过透射电镜(TEM)、扫描电镜(SEM)和能谱仪(EDS)观察并分析微生物表面情况,利用X射线衍射(XRD)分析手段测定铁锰结核矿物组成的变化。实验进行1天内细菌处于对数生长期,有菌组的Fe、Mn等离子浓度增加; 2—7天内细菌处于稳定期, Fe、Mn等离子浓度有一定程度降低,但总体浓度均大于无菌组的离子浓度,金属离子被吸附在菌体表面,新形成了简单的含Fe化合物和矿物;实验结束后,XRD分析结果显示样品的矿物含量,如菱铁矿、赤铁矿和针铁矿等有轻微程度的增加。研究表明盐场海芽孢杆菌(Marinibacilluscampisalis)能够促进释放铁锰结核中的Fe、Mn等元素,同时对释放出的金属离子又有富集作用,并能够诱导新矿物的形成。本研究为深入了解铁锰结核的生物成因提供了新的依据。  相似文献   

19.
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20.
Arsenic levels (up to 130 mg kg−1) substantially exceeding the official threshold have recently been documented in beach and nearshore sediments along more than 50 km of coastline in the Brazilian state of Espírito Santo between 19°50′ and 20°12′S. In an attempt to assess the sources of this enrichment, we performed a study on arsenic distribution in the main mineral substances and living organisms in the beach environment. Laboratory tests on arsenic retention by beach carbonate debris have also been carried out. The data suggest that sedimentary arsenic occurs largely bound to particles of the calcareous red alga Corallina panizzoi, whereby live specimens contained much smaller amounts of this metalloid than was the case for nonliving material (2.4 and 20.3 mg kg−1, respectively). Experimental tests confirmed the ability of C. panizzoi detritus to retain arsenic at pH intervals and ionic strength characteristic of seawater. There are two potential sources of that metalloid for calcareous debris in sediments: brown macroalgae, which were found to contain high levels of As (up to 66.3 mg kg−1), and ferruginized sandstones (up to 23.0 mg kg−1). We argue that any contribution of brown algae to beach sediment enrichment by As would be minor, and consider the ferrous sandstones from coastal sedimentary rocks of the Barreiras Group as the principal large-scale source of arsenic in the marine environment of Espírito Santo. The experimental data, together with field studies, corroborate the interpretation that arsenic anomalies in sediments with calcareous debris can form when weathered continental rocks even only slightly enriched in As are leached by marine waters, and the As is at least partially retained by biogenic calcareous detritus in nearshore sediments. Considering that rocks of the Barreiras Group are exposed to marine erosion far to the north of Espírito Santo, we estimate that marine sediments containing calcareous material are “anomalously” enriched in As along approximately 2,000 km of the Brazilian tropical coastline.  相似文献   

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